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Three-dose vaccination-induced immune responses protect against SARS-CoV-2 Omicron-BA.2

Runhong Zhou, Na Liu, Xin Li, Qiaoli Peng, Cheuk-Kwan Yiu, Haode Huang, Dawei Yang, Zhenglong Du, Hau-Yee Kwok, Ka-Kit Au, Jian-Piao Cai, Ivan Fan-Ngai Hung, Kelvin Kai-Wang To, Xiaoning Xu, Kwok-Yung Yuen, Zhiwei Chen
doi: https://doi.org/10.1101/2022.05.09.491254
Runhong Zhou
1AIDS Institute, Li Ka Shing Faculty of Medicine, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
2Department of Microbiology, Li Ka Shing Faculty of Medicine, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
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Na Liu
1AIDS Institute, Li Ka Shing Faculty of Medicine, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
2Department of Microbiology, Li Ka Shing Faculty of Medicine, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
6Department of Clinical Microbiology and Infection Control, the University of Hong Kong-Shenzhen Hospital; Shenzhen, Guangdong, People’s Republic of China
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Xin Li
2Department of Microbiology, Li Ka Shing Faculty of Medicine, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
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Qiaoli Peng
1AIDS Institute, Li Ka Shing Faculty of Medicine, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
2Department of Microbiology, Li Ka Shing Faculty of Medicine, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
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Cheuk-Kwan Yiu
3Department of Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, People’s Republic of China
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Haode Huang
1AIDS Institute, Li Ka Shing Faculty of Medicine, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
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Dawei Yang
1AIDS Institute, Li Ka Shing Faculty of Medicine, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
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Zhenglong Du
1AIDS Institute, Li Ka Shing Faculty of Medicine, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
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Hau-Yee Kwok
1AIDS Institute, Li Ka Shing Faculty of Medicine, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
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Ka-Kit Au
1AIDS Institute, Li Ka Shing Faculty of Medicine, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
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Jian-Piao Cai
2Department of Microbiology, Li Ka Shing Faculty of Medicine, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
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Ivan Fan-Ngai Hung
3Department of Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, People’s Republic of China
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Kelvin Kai-Wang To
2Department of Microbiology, Li Ka Shing Faculty of Medicine, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
4State Key Laboratory for Emerging Infectious Diseases, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
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Xiaoning Xu
7Centre for Immunology & Vaccinology, Chelsea and Westminster Hospital, Department of Medicine, Imperial College London, London, United Kingdom
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Kwok-Yung Yuen
2Department of Microbiology, Li Ka Shing Faculty of Medicine, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
4State Key Laboratory for Emerging Infectious Diseases, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
5Centre for Virology, Vaccinology and Therapeutics Limited, the University of Hong Kong, Hong Kong Special Administrative Region, People’s Republic of China
6Department of Clinical Microbiology and Infection Control, the University of Hong Kong-Shenzhen Hospital; Shenzhen, Guangdong, People’s Republic of China
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Zhiwei Chen
1AIDS Institute, Li Ka Shing Faculty of Medicine, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
2Department of Microbiology, Li Ka Shing Faculty of Medicine, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
4State Key Laboratory for Emerging Infectious Diseases, the University of Hong Kong; Pokfulam, Hong Kong Special Administrative Region, People’s Republic of China
5Centre for Virology, Vaccinology and Therapeutics Limited, the University of Hong Kong, Hong Kong Special Administrative Region, People’s Republic of China
6Department of Clinical Microbiology and Infection Control, the University of Hong Kong-Shenzhen Hospital; Shenzhen, Guangdong, People’s Republic of China
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  • For correspondence: zchenai@hku.hk
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Summary

The ongoing outbreak of SARS-CoV-2 Omicron BA.2 infections in Hong Kong, the world model city of universal masking, has resulted in a major public health crisis. In this study, we investigate public servants who had been vaccinated with two dose (82.7%) or three dose (14%) of either CoronaVac (CorV) or BNT162b2 (BNT). During the BA.2 outbreak, 29.3% vaccinees were infected. Three-dose vaccination provided protection with lower incidence rates of breakthrough infections (2×BNT 49.2% vs 3×BNT 16.6%, p<0.0001; 2×CorV 48.6% vs 3×CoV 20.6%, p=0.003). The third heterologous vaccination showed the lowest incidence (2×CorV+1×BNT 6.3%). Although BA.2 conferred the highest neutralization resistance compared with variants of concern tested, the third dose vaccination-activated spike-specific memory B and Omicron cross-reactive T cell responses contributed to reduced frequencies of breakthrough infection and disease severity. Our results have implications to timely boost vaccination and immune responses likely required for vaccine-mediated protection against Omicron BA.2 pandemic.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • ↵9 Lead contact.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted May 11, 2022.
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Three-dose vaccination-induced immune responses protect against SARS-CoV-2 Omicron-BA.2
Runhong Zhou, Na Liu, Xin Li, Qiaoli Peng, Cheuk-Kwan Yiu, Haode Huang, Dawei Yang, Zhenglong Du, Hau-Yee Kwok, Ka-Kit Au, Jian-Piao Cai, Ivan Fan-Ngai Hung, Kelvin Kai-Wang To, Xiaoning Xu, Kwok-Yung Yuen, Zhiwei Chen
bioRxiv 2022.05.09.491254; doi: https://doi.org/10.1101/2022.05.09.491254
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Three-dose vaccination-induced immune responses protect against SARS-CoV-2 Omicron-BA.2
Runhong Zhou, Na Liu, Xin Li, Qiaoli Peng, Cheuk-Kwan Yiu, Haode Huang, Dawei Yang, Zhenglong Du, Hau-Yee Kwok, Ka-Kit Au, Jian-Piao Cai, Ivan Fan-Ngai Hung, Kelvin Kai-Wang To, Xiaoning Xu, Kwok-Yung Yuen, Zhiwei Chen
bioRxiv 2022.05.09.491254; doi: https://doi.org/10.1101/2022.05.09.491254

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